Art

J-GLOBAL ID：200902286133409940   Reference number：09A0112103

Characterization of the Kyoto Circling (KCI) Rat Carrying a Spontaneous Nonsense Mutation in the Protocadherin 15 (Pcdh15) Gene

プロトカドヘリン15(Pcdh15)遺伝子に自発性ナンセンス変異があるKyoto Circling(KCI)ラットの特徴付け

Author (7)： NAOI Kuniko (Inst. of Lab. Animals, Graduate School of Medicine, Kyoto Univ.) ,  NAOI Kuniko (Dep. of Medical Therapeutics, Molecular Therapeutics, Gifu Pharmaceutical Univ.) ,  KURAMOTO Takashi (Inst. of Lab. Animals, Graduate School of Medicine, Kyoto Univ.) ,  KUWAMURA Yuki (Osaka Pathology Center, Drug Safety Res. Laboratories, Shin Nippon Biomedical Laboratories, LTD.) ,  GOHMA Hiroshi (Inst. of Lab. Animals, Graduate School of Medicine, Kyoto Univ.) ,  KUWAMURA Mitsuru (Lab. of Veterinary Pathology, Osaka Prefecture Univ.) ,  SERIKAWA Tadao (Inst. of Lab. Animals, Graduate School of Medicine, Kyoto Univ.)
Material： Experimental Animals  (実験動物ニュース)
Volume： 58  Issue： 1  Page： 1-10 (J-STAGE)  Publication year： 2009 
JST Material Number： Z0755A  ISSN： 1341-1357  Document type： Article
Article type： 原著論文  Country of issue： Japan (JPN)  Language： ENGLISH (EN)

Thesaurus term： *cell adhesion molecule ,...
Semi thesaurus term： RFLP ,...

Register(free) or Log In to access     To see more with JDream III (charged).   {{ this.onShowAbsJLink("http://jdream3.com/lp/jglobal/index.html?docNo=09A0112103&from=J-GLOBAL&jstjournalNo=Z0755A") }}

JST classification (4)： Auditory sense  (EJ13030M) ,  Genetic variation  (EC01030Y) ,  Laboratry organisms  (EA03070Y) ,  Basic otorhinolaryngology  (GQ01020F)

Reference (18)：

• AHITUV, N. Mouse models for human deafness : current tools for new fashions. Trends Mol. Med. 2002, 8, 447-451
• AHMED, Z. M. Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F. Am. J. Hum. Genet. 2001, 69, 25-34
• AHMED, Z. M. PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23. Hum. Mol. Genet. 2003, 12, 3215-3223
• ALAGRAMAM, K. N. Neuroepithelial defects of the inner ear in a new allele of the mouse mutation Ames waltzer. Hear. Res. 2000, 148, 181-191
• ALAGRAMAM, K. N. The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene. Nat. Genet. 2001, 27, 99-102

Terms in the title (5)： プロトカドヘリン ,  遺伝子 ,  自発性 ,  ナンセンス変異 ,  ラット